Total synthesis of (-)-reveromycin A via a hetero-Diels-Alder approach

Synthesis

Volumn , Issue 23, 2010, Pages 3954-3966

  El Sous, Mariana ^a   Ganame, Danny ^a   Tregloan, Peter ^a   Rizzacasa, Mark A ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

6,6 spiroketal; hetero Diels Alder; high pressure acylation; reveromycin; Stille coupling

Indexed keywords

[6,6]-SPIROKETAL; HETERO-DIELS-ALDER; HIGH-PRESSURE ACYLATION; REVEROMYCIN; STILLE COUPLING;

ACIDS; ACYLATION; CONDENSATION REACTIONS; STEREOCHEMISTRY;

SYNTHESIS (CHEMICAL);

1 (BENZYLOXY) 3 METHYLENEHEPTAN 2 OL; 1 (BENZYLOXY) 3 METHYLENEHEPTAN 2 ONE; 2 (2 TRIMETHYLSILYLETHYLTHIO)ETHYLAMINE; 5 6 SPIROKETAL; ACETONITRILE; ALCOHOL; ALDOL ADDUCT; ALKENE; ANTIFUNGAL AGENT; DICYCLOHEXYLCARBODIIMIDE; DIENE ESTER; DIOL; REAGENT; REVEROMYCIN A; SPIROKETAL; SPIROKETAL ALKYNE; STANNANE; SUCCINATE ESTER; TETRABUTYLAMMONIUM; TRIACETATE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHEMICAL REACTION; CROSS COUPLING REACTION; DESS MARTIN OXIDATION; DIELS ALDER REACTION; DRUG DEGRADATION; DRUG SYNTHESIS; ISOMERIZATION; STEREOCHEMISTRY; THERMODYNAMICS; WITTIG REACTION;

EID: 78650075664     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258308     Document Type: Article

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